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从非聚乙二醇化干扰素β-1a转换为聚乙二醇化干扰素β-1a的患者出现新的流感样症状的风险较低:ALLOW 3b期试验结果。

Patients transitioning from non-pegylated to pegylated interferon beta-1a have a low risk of new flu-like symptoms: ALLOW phase 3b trial results.

作者信息

Naismith Robert T, Hendin Barry, Wray Sibyl, Huang DeRen, Gaudenzi Fiorenza, Dong Qunming, Sperling Bjørn, Mann Monica, Werneburg Brian

机构信息

Department of Neurology, Washington University in St Louis, USA.

Phoenix Neurological Associates, USA.

出版信息

Mult Scler J Exp Transl Clin. 2019 Jan 30;5(1):2055217318822148. doi: 10.1177/2055217318822148. eCollection 2019 Jan-Mar.

Abstract

BACKGROUND

Flu-like symptoms are common adverse events associated with interferon beta relapsing multiple sclerosis therapies.

OBJECTIVES

To evaluate the incidence and severity of flu-like symptoms after transitioning from non-pegylated interferons to peginterferon beta-1a and assess flu-like symptom mitigation using naproxen.

METHODS

ALLOW was a phase 3b open-label study in relapsing multiple sclerosis patients. Patients had received non-pegylated interferon for 4 or more months immediately before beginning a 4-week screening period. At baseline, patients switched to peginterferon beta-1a and were randomly assigned (1:1) to continue their current flu-like symptoms management regimen or start twice-daily naproxen 500 mg for 8 weeks. Patients then switched to their preferred regimen and were followed for 48 weeks in total.

RESULTS

Of 201 patients, 89.6% did not experience new/worsening flu-like symptoms during their first 8 weeks on peginterferon beta-1a. Flu-like symptom severity remained low in current-regimen and naproxen patients, with no significant between-group differences. Median flu-like symptom duration per injection was 3.2 hours longer with peginterferon beta-1a versus prior interferon, but the 4-week cumulative duration was reduced 49-78%. No new safety signals were identified.

CONCLUSION

Most patients who switched from non-pegylated interferon to peginterferon beta-1a did not experience new/worsening flu-like symptoms. Flu-like symptom duration per injection increased, but the cumulative duration significantly decreased. These data may inform flu-like symptom management guidance.

摘要

背景

流感样症状是与β-干扰素治疗复发型多发性硬化症相关的常见不良事件。

目的

评估从非聚乙二醇化干扰素转换为聚乙二醇化β-1a干扰素后流感样症状的发生率和严重程度,并评估使用萘普生减轻流感样症状的效果。

方法

ALLOW是一项针对复发型多发性硬化症患者的3b期开放标签研究。患者在开始为期4周的筛查期之前,已接受非聚乙二醇化干扰素治疗4个月或更长时间。在基线时,患者转换为聚乙二醇化β-1a干扰素,并被随机分配(1:1)继续其当前的流感样症状管理方案,或开始每日两次服用500毫克萘普生,持续8周。然后患者转换为他们喜欢的方案,并总共随访48周。

结果

在201例患者中,89.6%在开始使用聚乙二醇化β-1a干扰素的前8周内未出现新的/加重的流感样症状。当前方案组和萘普生组患者的流感样症状严重程度仍然较低,组间无显著差异。与先前的干扰素相比,聚乙二醇化β-1a干扰素每次注射的流感样症状中位持续时间长3.2小时,但4周累计持续时间减少了49-78%。未发现新的安全信号。

结论

大多数从非聚乙二醇化干扰素转换为聚乙二醇化β-1a干扰素的患者未出现新的/加重的流感样症状。每次注射的流感样症状持续时间增加,但累计持续时间显著减少。这些数据可为流感样症状管理指导提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09c0/6354308/9642464b8cbe/10.1177_2055217318822148-fig1.jpg

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